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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7406Erstellt: 23. Oktober 2026

Hexane → 1-Benzyl-4-(1-phenethyl-1H-imidazol-2-YL)piperidin-4-OL

https://huagongshe.com/de/reaction/7406

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHexaneHCID 8058—
Edukt1-Benzyl-4-piperidoneHCID 19220—
Edukt1-(1-Phenylethyl)-1h-imidazoleHCID 9815351—
EduktButyllithiumHCID 178418339—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-Benzyl-4-(1-phenethyl-1H-imidazol-2-YL)piperidin-4-OLHCID 1132590475%

Reaktionsbedingungen

Temperatur-70 °C

Reaktionsschritte

A mixture of DIPA (1.4 mol) in THF (3000 ml) was stirred at −70° C. under N2 flow. Butyllithium 2.5 M/hexane (1.3 mol) was added portionwise at a temperature below −40° C. The mixture was stirred at −70° C. for 15 min. 1-phenylethyl-1H-imidazole (1 mol) dissolved in THF was added dropwise at a temperature below −55° C. The mixture was stirred at −70° C. for 1 hour. 1-(phenylmethyl)-4-piperidinone (1.2 mol) dissolved in THF was added dropwise at a temperature below −55° C. The mixture was stirred at −70° C. for 1 hour, then brought to room temperature, stirred at room temperature overnight and decomposed with H2O. The organic solvent was evaporated. The aqueous concentrate was extracted with CH2Cl2. The organic layer was separated, dried (MgSO4), filtered and the solvent was evaporated. The residue was crystallized from DIPE (1100 ml). The precipitate was filtered off, washed with DIPE and dried, yielding 271 g of 4-[1-(2-phenylethyl)-1H-imidazol-2-yl]-1-(phenylmethyl)-4-piperidinol (75%) (interm. 1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07087595B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-b62c82ce4a9f497c902d1d7f12e1a2c2
Quellennotizuspto-grants-2006_08